CELESTONE SOLUSPAN (Merck Sharp & Dohme Corp.)


Welcome to the PulseAid listing for the CELESTONE SOLUSPAN drug offered from Merck Sharp & Dohme Corp.. This Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
LABELER NAME / MANUFACTURER: Merck Sharp & Dohme Corp.
NON-PROPRIETARY NAME: Betamethasone Acetate and Betamethasone Sodium Phosphate
SUBSTANCE NAME: BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE
TYPE: HUMAN PRESCRIPTION DRUG
PHARMA CLASS: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
ROUTE: INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE
DOSAGE FORM: INJECTION, SUSPENSION
MARKETING CATEGORY NAME: NDA
START MARKETING DATE: 1965-03-15
END MARKETING DATE: 0000-00-00


CELESTONE SOLUSPAN HUMAN PRESCRIPTION DRUG Details:

Item DescriptionCELESTONE SOLUSPAN from Merck Sharp & Dohme Corp.
LABELER NAME: Merck Sharp & Dohme Corp.
DEA SCHEDULE:
ACTIVE STRENGTH: 3; 3(mg/mL; mg/mL)
START MARKETING DATE: 1965-03-15
END MARKETING DATE: 0000-00-00
PRODUCT ID: 0085-0566_fba8e08c-0dcb-42ad-b443-53983b429473
PRODUCT NDC: 0085-0566
APPLICATION NUMBER: NDA014602

Other BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE Pharmaceutical Manufacturers / Labelers:

Manufacturer / LabelerProprietary Name
American Regent, Inc.Betamethasone Sodium Phosphate and Betamethasone Acetate
Merck Sharp & Dohme Corp.CELESTONE SOLUSPAN
PharmaForce, Inc.Betamethasone Sodium Phosphate and Betamethasone Acetate
REMEDYREPACK INC.Betamethasone Sodium Phosphate and Betamethasone Acetate
Terrain PharmaceuticalsReadySharp Betamethasone